Tag | Content |
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EnhancerAtlas ID | HS129-30008 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr5:138031900-138032880 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr5:138032454-138032464 | GGAAATCCCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29550 | chr5:138031242-138033269 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I138695 | chr5 | 138031404 | 138032863 |
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Enhancer Sequence | CGTCAACGGC TCCCATTTGG AGATGGCAGG CTATGGACCA GGCACAGTGC TGCACACTCT 60 AGAAGCATTA TGTCAGGAGG CTGAGGCAGG ACAATGGTGT GAACTCGGGA GGCGGAGCTT 120 GCAGTGAGCC AAGATCGCGC GACTGCACAC CAGCCTGGGC GACAGAGCAA GACTCCGTCT 180 CAAAAAAAAA AAAAAAAGAA GCATTATGTC ATCTCATTCT CACAACAGTT CCCTGAGACA 240 GGTATAATTA TCCCCACCTA ACAGATGAAG AAACAGGCTC AGTGAACAGA AGGCACTTGC 300 CAGGTGGTTT CTACTGCAAA GCTGTGATCT TTCTTCTGCA AGGAATTGCC TCTTTCCTAA 360 ACCTCCTGGC GCCTGGTTCC CAGCATGAGA ACTTGTGACT AAATGTAGGT GACGGGGGCC 420 TATGGCGGCC CTTCTGTGGC AGCCAATGAG GGAGCAGGGT AAGGACCTGC CAGCTCAGGA 480 ACCTGCCCTC CATGAATCTG CCCCCAGTTC TTTCACAGCT GTGGGGAGAC ACCAAGCCCT 540 GAGTCACTTC CCTGGGAAAT CCCCGCAGAG GCTTTCCTGG GAATAAGATA ATGCAGGAAT 600 CTGGGCTGGA CTGTCCAAGG GGCCCGATTC CTGCCAGCCA GCCTATACGT CTTGGAGCAA 660 GACCTCAGGG TCTTCTCCAG ATATGGACAG GCCTGATAGA CATAAGCTGC AGTGGGACAA 720 GCAACATGTG TAGAAGGCCT CTGGAGAGAG GGGTCTGGGA AAGGGATGGG GTGGGTATCT 780 CTGCCATCAA GAGAATGATT GCTAAGGCTC CCTCCCAGGC CAAGGCAATG GCAACCTGTG 840 ATTCTGTGGG TCAGGGATGA GGCCACTTCA GTGAAAGGCC TTCAGCCTGA CCCCCCCGTA 900 GGAGACAGGG AGGCAAATGG CTGAGCAGAT GCCATGGCCG AGAACTCAGG TTAGAGGCCA 960 GTTACGGTGG CTCATGCCTG 980
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